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Magnetic Nanoparticles Create Hot Spots in Polymer Matrix for Controlled Drug Release

机译:磁性纳米粒子在聚合物基质中形成热点以控制药物释放

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摘要

Herein, original magnetic drug delivery nanomaterials for cancer therapy are developed and compared, with the purpose to show active control over drug release by using an alternative magnetic field (AMF). The rationale is to combine polymers and superparamagnetic nanoparticles to trigger such drug release under AMF. Two magnetic nanosystems are thus presented: magnetic nanogels made of thermosensitive and biocompatible polymers and core-shell nanoparticles with a magnetic core and a molecularly imprinted polymer as shell. Both encapsulate doxorubicin (DOX) and the DOX controlled release was investigated in vitro and in cells under AMF excitation. It confirms that the local heat profile at the vicinity of the iron oxide core can be used for the DOX controlled release. It also shows that both nanosystems help delivering more DOX inside the cells compared to internalization of free DOX. Finally, the DOX intracellular release could be remotely triggered under AMF, in athermal conditions, thus enhancing DOX cytotoxicity.
机译:在本文中,开发并比较了用于癌症治疗的原始磁性药物输送纳米材料,目的是通过使用替代磁场(AMF)来显示对药物释放的主动控制。基本原理是将聚合物和超顺磁性纳米粒子结合起来,以触发AMF下的此类药物释放。因此,提出了两种磁性纳米系统:由热敏性和生物相容性聚合物制成的磁性纳米凝胶,以及具有磁性核和分子印迹聚合物作为壳的核-壳纳米颗粒。封装的阿霉素(DOX)和DOX控释都在体外和在AMF激发下的细胞中进行了研究。这证实了氧化铁芯附近的局部热分布可用于DOX控释。它还表明,与自由DOX的内部化相比,这两种纳米系统都有助于在细胞内传递更多的DOX。最后,在无热条件下,AMF可以远程触发DOX的细胞内释放,从而增强DOX的细胞毒性。

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